These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

287 related articles for article (PubMed ID: 16986162)

  • 1. Imputation methods to improve inference in SNP association studies.
    Dai JY; Ruczinski I; LeBlanc M; Kooperberg C
    Genet Epidemiol; 2006 Dec; 30(8):690-702. PubMed ID: 16986162
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Accounting for haplotype uncertainty in matched association studies: a comparison of simple and flexible techniques.
    Kraft P; Cox DG; Paynter RA; Hunter D; De Vivo I
    Genet Epidemiol; 2005 Apr; 28(3):261-72. PubMed ID: 15637718
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Inference of missing SNPs and information quantity measurements for haplotype blocks.
    Su SC; Kuo CC; Chen T
    Bioinformatics; 2005 May; 21(9):2001-7. PubMed ID: 15699029
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Estimating haplotype frequencies and standard errors for multiple single nucleotide polymorphisms.
    Li SS; Khalid N; Carlson C; Zhao LP
    Biostatistics; 2003 Oct; 4(4):513-22. PubMed ID: 14557108
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Simple estimates of haplotype relative risks in case-control data.
    French B; Lumley T; Monks SA; Rice KM; Hindorff LA; Reiner AP; Psaty BM
    Genet Epidemiol; 2006 Sep; 30(6):485-94. PubMed ID: 16755519
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fine mapping functional sites or regions from case-control data using haplotypes of multiple linked SNPs.
    Cheng R; Ma JZ; Elston RC; Li MD
    Ann Hum Genet; 2005 Jan; 69(Pt 1):102-12. PubMed ID: 15638831
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Haplotype uncertainty in association studies.
    Mensah FK; Gilthorpe MS; Davies CF; Keen LJ; Adamson PJ; Roman E; Morgan GJ; Bidwell JL; Law GR
    Genet Epidemiol; 2007 May; 31(4):348-57. PubMed ID: 17323369
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Haplotype association analysis for late onset diseases using nuclear family data.
    Li C; Boehnke M
    Genet Epidemiol; 2006 Apr; 30(3):220-30. PubMed ID: 16470533
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Imputing missing genotypic data of single-nucleotide polymorphisms using neural networks.
    Sun YV; Kardia SL
    Eur J Hum Genet; 2008 Apr; 16(4):487-95. PubMed ID: 18197192
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evaluating the ability of tree-based methods and logistic regression for the detection of SNP-SNP interaction.
    García-Magariños M; López-de-Ullibarri I; Cao R; Salas A
    Ann Hum Genet; 2009 May; 73(Pt 3):360-9. PubMed ID: 19291098
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Conditional likelihood methods for haplotype-based association analysis using matched case-control data.
    Chen J; Rodriguez C
    Biometrics; 2007 Dec; 63(4):1099-107. PubMed ID: 18078481
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Using tree-based recursive partitioning methods to group haplotypes for increased power in association studies.
    Yu K; Xu J; Rao DC; Province M
    Ann Hum Genet; 2005 Sep; 69(Pt 5):577-89. PubMed ID: 16138916
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Inference of haplotype effects in case-control studies using unphased genotype and environmental data.
    Chen X; Li Z
    Biom J; 2008 Apr; 50(2):270-82. PubMed ID: 18217697
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Accurate haplotype inference for multiple linked single-nucleotide polymorphisms using sibship data.
    Liu PY; Lu Y; Deng HW
    Genetics; 2006 Sep; 174(1):499-509. PubMed ID: 16783022
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Maximum-likelihood estimation of haplotype frequencies in nuclear families.
    Becker T; Knapp M
    Genet Epidemiol; 2004 Jul; 27(1):21-32. PubMed ID: 15185400
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An expectation-maximization-likelihood-ratio test for handling missing data: application in experimental crosses.
    Niu T; Ding AA; Kreutz R; Lindpaintner K
    Genetics; 2005 Feb; 169(2):1021-31. PubMed ID: 15731519
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Disease association tests by inferring ancestral haplotypes using a hidden markov model.
    Su SY; Balding DJ; Coin LJ
    Bioinformatics; 2008 Apr; 24(7):972-8. PubMed ID: 18296746
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Haplotype association analysis of human disease traits using genotype data of unrelated individuals.
    Tan Q; Christiansen L; Christensen K; Bathum L; Li S; Zhao JH; Kruse TA
    Genet Res; 2005 Dec; 86(3):223-31. PubMed ID: 16454861
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Haplotype inference for population data with genotyping errors.
    Zhu W; Kuk AY; Guo J
    Biom J; 2009 Aug; 51(4):644-58. PubMed ID: 19688759
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel method to express SNP-based genetic heterogeneity, Psi, and its use to measure linkage disequilibrium for multiple SNPs, D(g), and to estimate absolute maximum of haplotype frequency.
    Yamada R; Matsuda F
    Genet Epidemiol; 2007 Nov; 31(7):709-26. PubMed ID: 17508358
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.